Canonical Allele Identifier: PA2580503419
Gene: COL11A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2115442
ClinVar RCV Id: RCV003032663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542411.2:p.Cys1655Gly
CA363616216
NM_080680.3:c.4963T>G